Predicted protein targets (top 5)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | NOS3 | P29474 | 1/20 | 0.34 |
| ▸ | NOS2 | P35228 | 1/20 | 0.34 |
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.32 |
| ▸ | TSHR | P16473 | 1/20 | 0.32 |
| ▸ | RAPGEF4 | Q8WZA2 | 1/20 | 0.31 |
Click a target to see other patent compounds predicted against it — the reverse direction, in place.
Similar compounds — the chemically nearest patent molecules
Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| SCHEMBL27903407 | 0.88 | TPMT (0.30) | — | |
| SCHEMBL466431 | 0.87 | NOS3 (0.31) | NOS3NOS2 | |
| Lithium Ion SCHEMBL752492 | 0.84 | — | — | |
| SCHEMBL456834 | 0.83 | — | — | |
| SCHEMBL457435 | 0.83 | — | — | |
| SCHEMBL9139369 | 0.79 | TP53 (0.41) | TSHRRAPGEF4 | |
| SCHEMBL456298 | 0.79 | ACHE (0.37) | — | |
| SCHEMBL1780256 | 0.78 | NOS2 (0.39) | NOS3NOS2ALDH1A1 | |
| SCHEMBL457229 | 0.78 | — | — | |
| SCHEMBL509320 | 0.78 | — | — |
Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.
Patent provenance — the patents this molecule appears in, and who filed them
Claimed or disclosed in 288 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-114423739-B | Improved enantioselective hydrogenation of 4-substituted 1, 2-dihydroquinolines in the presence of chiral iridium catalysts and additives | 拜耳公司 | 2024-06-25 | — | — | CN | claimed |
| CN-114514223-B | Process for enantioselective hydrogenation of 4-substituted 1, 2-dihydroquinolines comprising using novel iridium catalysts | 拜耳公司 | 2024-05-17 | — | — | CN | claimed |
| CN-111902399-B | Enantioselective hydrogenation of 4-substituted 1, 2-dihydroquinolines in the presence of chiral iridium catalysts | 拜耳公司 | 2023-11-28 | — | — | CN | claimed |
| WO-2023172667-A2 | SUBSTITUTED IMIDAZO[1,5-a]PYRIDINE N-HETEROCYCLIC CARBENE (NHC) LIGANDS, CATALYST COMPLEXES THEREOF, AND METHODS USING SAME | RUTGERS, THE STATE UNIVERSITY OF NEW JERSEY (US) | 2023-09-14 | — | — | WO | claimed |
| EP-3774735-B1 | ENANTIOSELECTIVE HYDROGENATION OF 4-SUBSTITUTED 1,2-DIHYDROQUINOLINES IN PRESENCE OF A CHIRAL IRIDIUM CATALYST | BAYER AG (DE) | 2023-09-13 | — | — | EP | claimed |
| CN-116693734-A | Preparation method and application of trans-1, 2-poly-ocimene | 湖北航天化学技术研究所 | 2023-09-05 | — | — | CN | claimed |
| CN-116693733-A | Isotactic cis-1, 4-poly-ocimene and preparation method and application thereof | 中国科学院长春应用化学研究所 | 2023-09-05 | — | — | CN | claimed |
| CN-116554372-A | Preparation method of low-entanglement ultra-high molecular weight polyethylene | 中国科学院长春应用化学研究所 | 2023-08-08 | — | — | CN | claimed |
| EP-4034528-A1 | PROCESS COMPRISING THE USE OF NEW IRIDIUM CATALYSTS FOR ENANTIOSELECTIVE HYDROGENATION OF 4-SUBSTITUTED 1,2-DIHYDROQUINOLINES | Bayer Aktiengesellschaft (DE) | 2022-08-03 | — | — | EP | claimed |
| CN-114514223-A | Process comprising enantioselective hydrogenation of 4-substituted 1, 2-dihydroquinolines using a novel iridium catalyst | 拜耳公司 | 2022-05-17 | — | — | CN | claimed |
| EP-2289949-A1 | ISOPRENE OR BUTADIENE CIS 1,4-POLYMERIC BI-COMPONENT CATALYST SYSTEM AND POLYMERIZATION PROCESS | Changchun Institute Of Applied Chemistry Chinese Academy Of Sciences (CN) | 2011-03-02 | — | — | EP | claimed |
| US-20100286350-A1 | BI-COMPONENT CATALYST SYSTEM FOR ISOPRENE OR BUTADIENE CIS 1, 4-POLYMERIZATION AND POLYMERIZATION PROCESS | CHANGCHUN INSTITUTE OF APPLIED CHEMISTRY CHINESE ACADEMY OF SCIENCES (CN) | 2010-11-11 | — | — | US | claimed |
| US-20080139830-A1 | Preparation of substituted aminoanthraquinones | LANXESS DEUTSCHLAND GMBH | 2008-06-12 | — | — | US | claimed |
| EP-1930377-A2 | Method for producing substituted aminoanthraquinones | Lanxess Deutschland GmbH (DE) | 2008-06-11 | — | — | EP | claimed |
| EP-0797774-A1 | MULTILAYER ANALYTICAL ELEMENT | 2860601 Canada Inc. (CN) | 1997-10-01 | — | — | EP | claimed |
| WO-1996018898-A1 | MULTILAYER ANALYTICAL ELEMENT | 2860601 CANADA INC. (CA) | 1996-06-20 | — | — | WO | claimed |
| EP-0312019-B1 | CONDENSED HETEROCYCLIC COMPOUNDS, A PROCESS FOR PREPARING THE SAME AND A HERBICIDAL COMPOSITION THEREOF | DAICEL CHEMICAL INDUSTRIES, LTD. (JP) | 1993-08-04 | — | — | EP | claimed |
| US-4936121-A | Condensed heterocyclic compounds, a process for preparing the same and a herbicidal composition thereof | DAICEL CHEMICAL INDUSTRIES LTD. (JP) | 1990-06-26 | — | — | US | claimed |
| EP-0312019-A2 | Condensed heterocyclic compounds, a process for preparing the same and a herbicidal composition thereof | DAICEL CHEMICAL INDUSTRIES, LTD. (JP) | 1989-04-19 | — | — | EP | claimed |
| US-4585574-A | POSITIVE DIELECTRIC ANISOTROPY | BAYER AKTIENGESELLSCHAFT (DE) | 1986-04-29 | — | — | US | claimed |